Canonical Allele Identifier: CA2154484068
Gene: CALM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.90404394A= , CM000676.2:g.90404394A= GRCh38
NC_000014.8:g.90870738A= , CM000676.1:g.90870738A= GRCh37
NC_000014.7:g.89940491A= NCBI36
NG_013338.1:g.12412A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356978.9:c.301A= MANE Select ENSP00000349467.4:p.Ile101=
ENST00000447653.8:c.193A= ENSP00000403491.4:p.Ile65=
ENST00000659177.1:c.193A= ENSP00000499421.1:p.Ile65=
ENST00000663135.1:c.193A= ENSP00000499498.1:p.Ile65=
ENST00000356978.8:c.301A= ENSP00000349467.4:p.Ile101=
ENST00000447653.7:c.304A= ENSP00000403491.3:p.Ile102=
ENST00000544280.6:c.193A= ENSP00000442853.2:p.Ile65=
ENST00000553422.1:c.178-5A= ENSP00000450425.1:n.178-5A=
ENST00000553542.5:c.193A= ENSP00000450829.1:p.Ile65=
ENST00000553630.1:c.194A= ENSP00000451646.1:p.Tyr65=
ENST00000553964.5:n.2431A=
ENST00000554296.1:n.353A=
ENST00000556721.1:n.227A=
ENST00000557020.5:c.193A= ENSP00000451062.1:p.Ile65=
ENST00000626705.2:c.166-63A= ENSP00000486402.1:n.166-63A=
NM_006888.4:c.301A= NP_008819.1:p.Ile101=
XM_006720258.2:c.304A= XP_006720321.1:p.Ile102=
NM_001363669.1:c.193A= NP_001350598.1:p.Ile65=
NM_001363670.1:c.304A= NP_001350599.1:p.Ile102=
NM_006888.5:c.301A= NP_008819.1:p.Ile101=
NM_006888.6:c.301A= MANE Select NP_008819.1:p.Ile101=
NM_001363669.2:c.193A= NP_001350598.1:p.Ile65=
NM_001363670.2:c.304A= NP_001350599.1:p.Ile102=